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ImmunoWELL Cardiolipin (IgG) Test

FDA UDI

Class II (US FDA UDI)

by Genbio

Identity

Trade Name
ImmunoWELL Cardiolipin (IgG) Test FDA UDI
Generic Name
Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The ImmunoWELL Cardiolipin Antibody (IgG) Test is an enzyme immunoassay (EIA) for the quantitative detection of antibodies to cardiolipin antigen in serum and is used as an aid for assessing the risk of thrombosis in individuals with systemic lupus erythematosus (SLE) and lupus-like disorders. FDA UDI
Model / Reference
800-3090 FDA UDI
Description
The ImmunoWELL Cardiolipin Antibody (IgG) Test is an enzyme immunoassay (EIA) for the quantitative detection of antibodies to cardiolipin antigen in serum and is used as an aid for assessing the risk of thrombosis in individuals with systemic lupus erythematosus (SLE) and lupus-like disorders. FDA UDI

Identifiers

Catalog Number
3090 FDA UDI
Primary DI / UDI-DI
00613745030906 FDA UDI
FDA Product Code
MID FDA UDI
GMDN Term
Anticardiolipin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5660 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

ImmunoWELL Cardiolipin (IgG) Test by Genbio — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Genbio

Sources (1)

  • FDA UDI 4c17cfad-23c1-4d2d-9802-ba17497a4485 38 fields · synced Jun 8, 2026